| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76047795-76048207 | Common:5; Rare:243 | ||||
| chr7:76303513-76303817 | Common:3; Rare:200; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:76359180-76359560 | Common:16; Rare:242 | ||||
| chr7:76392980-76393410 | Common:3; Rare:223 | ||||
| chr7:76409615-76409849 | Common:1; Rare:53 | ||||
| chr7:77122187-77122778 | Common:4; Rare:194 | ||||
| chr7:77415977-77416457 | Common:2; Rare:254 | ||||
| chr7:77536816-77537204 | Common:8; Rare:223 | ||||
| chr7:77696132-77696521 | Common:2; Rare:298 | ||||
| chr7:77696980-77697098 | Common:1; Rare:46 | ||||
| chr7:77697271-77697780 | Common:2; Rare:175 | ||||
| chr7:77798347-77798906 | Common:2; Rare:261 | ||||
| chr7:79452704-79453004 | Common:1; Rare:96 | ||||
| chr7:79453084-79453480 | Common:3; Rare:136; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:79453394-79454106 | Common:7; Rare:316 |